Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Axenfeld-Rieger syndrome type 2 (DOID:0110121)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
10p Deletion Syndrome (partial) 
16p11.2 Deletion Syndrome  
1q24 Deletion Syndrome  
22q11 Deletion Syndrome +   
3p deletion syndrome 
46,XY sex reversal 10  
46,XY sex reversal 4  
ADULT syndrome  
Aloi Tomasini Isaia Syndrome 
alpha thalassemia-intellectual disability syndrome type 1 
AMME complex  
Anodontia of Permanent Dentition 
Axenfeld-Rieger Anomaly with Cardiac Defects and Sensorineural Hearing Loss 
Axenfeld-Rieger syndrome type 1  
Axenfeld-Rieger syndrome type 2 
An Axenfeld-Rieger syndrome that has_material_basis_in deletions in the region 13q14. (DO)
Axenfeld-Rieger syndrome type 3  
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
chromosome 10q23 deletion syndrome  
Chromosome 11p Deletion Syndrome  
chromosome 13q14 deletion syndrome  
Chromosome 13q33-q34 Deletion Syndrome 
chromosome 14q11-q22 deletion syndrome 
chromosome 15q11.2 deletion syndrome  
chromosome 15q13.3 microdeletion syndrome  
Chromosome 15q14 Deletion Syndrome 
chromosome 15q24 deletion syndrome  
chromosome 15q25 deletion syndrome 
chromosome 15q26-qter deletion syndrome  
chromosome 16p11.2 deletion syndrome  
chromosome 16p12.1 deletion syndrome  
chromosome 16p12.2-p11.2 deletion syndrome 
chromosome 16q22 deletion syndrome  
Chromosome 17 Deletion  
chromosome 17p13.1 deletion syndrome 
chromosome 17q11.2 deletion syndrome  
chromosome 17q12 deletion syndrome  
chromosome 17q23.1-q23.2 deletion syndrome 
chromosome 18p deletion syndrome  
chromosome 18q deletion syndrome  
chromosome 19p13.13 deletion syndrome 
chromosome 19q13.11 deletion syndrome  
chromosome 1p36 deletion syndrome  
chromosome 1q21.1 deletion syndrome  
chromosome 1q41-q42 deletion syndrome +   
chromosome 2p12-p11.2 deletion syndrome 
chromosome 2p16.1-p15 deletion syndrome  
chromosome 2q31.2 deletion syndrome 
chromosome 2q37 deletion syndrome  
chromosome 3q13.31 deletion syndrome 
chromosome 3q29 microdeletion syndrome 
chromosome 4q21 deletion syndrome  
chromosome 5q deletion syndrome  
chromosome 5q12 deletion syndrome 
chromosome 6pter-p24 deletion syndrome 
chromosome 6q11-q14 deletion syndrome 
chromosome 6q24-q25 deletion syndrome 
chromosome 8q21.11 deletion syndrome 
chromosome 9p deletion syndrome  
chromosome Xp21 deletion syndrome 
Chromosome Xq21 Deletion Syndrome 
Cleft Palate, Deafness, and Oligodontia 
Cri-du-Chat syndrome +   
Deafness Oligodontia Syndrome 
Dermatoosteolysis Kirghizian Type 
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
distal 10q deletion syndrome  
Dysmyelinating Leukodystrophy with Oligodontia  
Ectodermal Dysplasia, Trichoodontoonychial Type 
GAPO syndrome  
Hao-Fountain Syndrome  
hereditary nonpolyposis colorectal cancer type 8  
Homozygous 11p15-p14 Deletion Syndrome 
Hypodontia Oligodontia with Orofacial Cleft 
hypohidrotic ectodermal dysplasia +   
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism  
hypoparathyroidism-deafness-renal disease syndrome  
hypotonia-cystinuria syndrome  
Jacobsen Syndrome +   
Kleefstra syndrome 1  
Koolen de Vries syndrome  
Late-Onset Localized Junctional Epidermolysis Bullosa with Mental Retardation 
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Maxillary Neoplasms +   
Mehta Lewis Patton Syndrome 
Microdontia Hypodontia Short Stature 
Miller-Dieker lissencephaly syndrome  
Monosomy 7 Myelodysplasia and Leukemia Syndrome +   
Nablus Mask-Like Facial Syndrome 
NFIA-related disorder  
Oligodontia-Colorectal Cancer Syndrome  
Phelan-McDermid syndrome  
Pinheiro Freire-Maia Miranda Syndrome 
posterior amorphous corneal dystrophy 
Potocki-Shaffer syndrome  
Rubinstein-Taybi syndrome +   
SATB2-associated syndrome  
Schopf-Schulz-Passarge syndrome  
SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY  
Smith-Magenis syndrome +   
solitary median maxillary central incisor  
Split-Hand and Split-Foot With Hypodontia 
Taurodontia, Absent Teeth, Sparse Hair 
Thai Symphalangism Syndrome 
thrombocytopenia-absent radius syndrome  
Thumb Deformity, Alopecia, Pigmentation Anomaly 
tooth and nail syndrome  
WAGR syndrome +   
Williams-Beuren syndrome +   
Wolf-Hirschhorn syndrome  
X-Linked Hypodontia 
Y-linked spermatogenic failure 1 
Zadik Barak Levin Syndrome 

Synonyms
Exact Synonyms: RIEG2 ;   Rieger syndrome 2 ;   Rieger syndrome type 2
Primary IDs: MESH:C535680
Alternate IDs: OMIM:601499
Xrefs: ICD10CM:Q13.8
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/8751862 "DO" "DO"

paths to the root